Rasagiline

Rasagiline

SCHEMBL333333

C#CCNC1CCc2ccccc21

nearest known ligand 1.00 ✓ in ChEMBL — recovers established targets

Full drug profile on Sugi Atlas →

Known targets — ChEMBL curated mechanism

MAOB

The experimentally established mechanism targets of Rasagiline. The predicted profile below is derived independently by chemical similarity — agreement is a validation signal, a miss is honest.

Predicted protein targets (top 9)

geneUniProtsupporting neighboursconfidence
MAOB known ✓ P27338 13/20 1.00
MAOA P21397 10/20 1.00
ACHE P22303 3/20 1.00
BCHE P06276 1/20 1.00
ADRA2B P18089 1/20 1.00
ADRA2C P18825 1/20 1.00
ADRA1A P35348 1/20 1.00
HTR6 P50406 1/20 1.00
PDPK1 O15530 1/20 0.59

Click a target to see other patent compounds predicted against it — the reverse direction, in place.

Similar compounds — the chemically nearest patent molecules

Nearest neighbours by Morgan-fingerprint cosine across the patent-compound collection, with each neighbour's top predicted target and the predicted targets it shares with this molecule.

Compoundsimilaritytop predictedshared targets
Rasagiline SCHEMBL74699 1.00 MAOB (1.00) MAOBMAOAACHEBCHEADRA2B
Azilect SCHEMBL332967 1.00 MAOB (1.00) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL2827373 1.00 MAOB (1.00) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL12787613 1.00 MAOB (1.00) MAOBMAOAACHEBCHEADRA2B
Azilect SCHEMBL29605291 1.00 MAOB (1.00) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL828802 0.98 MAOB (0.97) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL2028892 0.98 MAOB (0.97) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL5449858 0.98 MAOB (0.97) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL316969 0.98 MAOB (0.97) MAOBMAOAACHEBCHEADRA2B
Rasagiline SCHEMBL2349557 0.98 MAOB (0.97) MAOBMAOAACHEBCHEADRA2B

Similarity is cosine over the 2,048-bit Morgan fingerprint (≈ Tanimoto). Identical fingerprints score 1.00.

Patent provenance — the patents this molecule appears in, and who filed them

Claimed or disclosed in 606 patents — showing the first 20. claimed = in the patent's claims; disclosed = body only.

PatentTitleAssigneePublishedPriorityFilingCountryStatus
US-12310929-B2 Use of rasagiline for the treatment of restless legs syndrome TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 2025-05-27 US claimed
CN-110776429-B Improved preparation method of rasagiline racemic intermediate 齐鲁制药有限公司 2022-12-02 CN claimed
CN-110776429-A Improved preparation method of rasagiline racemic intermediate 齐鲁制药有限公司 2020-02-11 CN claimed
EP-2688561-B1 TRANSDERMAL COMPOSITIONS COMPRISING AN ACTIVE AGENT LAYER AND AN ACTIVE AGENT CONVERSION LAYER TEIKOKU PHARMA USA INC (US) 2018-08-22 EP claimed
US-9597301-B2 Propynylaminoindan transdermal compositions TEIKOKU PHARMA USA, INC. (US) 2017-03-21 US claimed
EP-1954667-B1 METHODS FOR ISOLATING PROPARGYLATED AMINOINDANS TEVA PHARMA (IL) 2017-02-08 EP claimed
EP-2563347-B1 PROPYNYLAMINOINDAN TRANSDERMAL COMPOSITIONS TEIKOKU PHARMA USA INC (US) 2016-10-12 EP claimed
US-20160184240-A1 Transdermal Compositions Comprising an Active Agent Layer and An Active Agent Conversion Layer TEIKOKU PHARMA USA, INC. 2016-06-30 US claimed
US-9119799-B2 Transdermal compositions comprising an active agent layer and an active agent conversion layer TEIKOKU PHARMA USA, INC. (US) 2015-09-01 US claimed
US-20150182476-A1 Propynylaminoindan Transdermal Compositions TEIKOKU SEIYAKU CO., LTD. (JP) 2015-07-02 US claimed
EP-0812190-A1 R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDAN, SALTS, COMPOSITIONS AND USES THEREOF TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 1997-12-17 EP claimed
EP-0538134-B1 Mono-fluorinated derivatives of N-propargyl-1-aminoindan and their use as inhibitors of monoamine oxidase TEVA PHARMA (IL) 1997-03-12 EP claimed
WO-1996037199-A1 USE OF R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDAN, SALTS, AND COMPOSITIONS THEREOF TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 1996-11-28 WO claimed
CN-1031995-C R-enantiomers of N-propargyl-1-aminoindan compounds, their preparation and pharmaceutical compositions containing them ORVET BV (NL) 1996-06-12 CN claimed
US-5457133-A Treating Parkinson's disease, memory disorders, Alzheimer's disease, depression and hyperactive syndrome TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 1995-10-10 US claimed
WO-1995011016-A1 R-ENANTIOMER OF N-PROPARGYL-1-AMINOINDAN, SALTS, COMPOSITIONS AND USES THEREOF TEVA PHARMACEUTICAL INDUSTRIES LTD. (IL) 1995-04-27 WO claimed
EP-0436492-B1 R-Enantiomer of N-propargyl-1-aminoindan, its preparation and pharmaceutical compositions containing it TEVA PHARMA (IL) 1994-06-08 EP claimed
EP-0538134-A2 Mono-fluorinated derivatives of N-propargyl-1-aminoindan and their use as inhibitors of monoamine oxidase TEVA PHARMACEUTICAL INDUSTRIES, LTD. (IL) 1993-04-21 EP claimed
CN-1062900-A The R-enantiomorph of N-propargyl-1-aminoidan, its method for making and contain its pharmaceutical composition ORVET BV (NL) 1992-07-22 CN claimed
EP-0436492-A2 R-Enantiomer of N-propargyl-1-aminoindan, its preparation and pharmaceutical compositions containing it Teva Pharmaceutical Industries Limited (IL) 1991-07-10 EP claimed

Patent text — is the patent's own abstract consistent with the prediction?

For each of this compound's patents that has machine-readable text (3 of them — usually the abstract, not the full specification), we ask MedCPT which protein the text reads most about, and where the chemistry-predicted target lands among 4885 human targets. A high rank means the patent's own wording is consistent with the prediction — a weak, independent signal, not proof of activity.

PatentTitleText reads most aboutPredicted target · text-rank
US-20150182476-A1 Propynylaminoindan Transdermal Compositions COL14A1, PNN, CUTA MAOB 3455/4885MAOA 2538/4885ACHE 566/4885
US-12310929-B2 Use of rasagiline for the treatment of restless legs syndrome RSU1, PRSS12, PNMT MAOB 748/4885MAOA 918/4885ACHE 533/4885
US-20160184240-A1 Transdermal Compositions Comprising an Active Agent Layer and An Active Agent Conversion Layer CUTA, S100A8, S100B MAOB 485/4885MAOA 332/4885ACHE 58/4885

“Text reads most about” is the patent abstract's nearest protein in MedCPT space (background-debiased). Only ~1.4% of patents have machine-readable text, so most compounds won't have this panel.